Polymerization chain-branching

Issues to be considered in selecting the best stabilizing system are polymeric chain branching which increases with high temperature and the presence of some stabilizers, polydispersity of the particles produced, and grafting copolymerization, which may occur because of the reaction of vinyl acetate with emulsifiers such as poly(vinyl alcohol) (43,44). 

Polymeric chain branching, 25 567—568 Polymeric composites, 13 369 Polymeric couplers, in chromogenic chemistry, 19 252... 

Chain branching in radical polymerization. Chain branching occurs when the growing end of a chain abstracts a hydrogen atom from the middle of a chain. A new branch grows off the chain at that point. 

From Equations 3.43-3.45 it follows that the condition = D is realised only at the following values of the indicated dimensions D 1.67, d = 1.0 and d = 1.0. The last condition means that the microgel is formed by a linear macromolecule [35]. However, as the curing process proceeds polymeric chain branching occurs and this results in d growth [35]. In turn, as follows from Equation 3.45, this will cause a corresponding increase in d,. In order to accept as d this dimension value for a branched polymer chain d = 1.33 [35]) and as d this dimension value determined for the cluster-cluster aggregates formed by the mechanism in computer simulation (J, = 1.42 [67]), then Equation 3.43 can be written as follows [66] ... 

Chain transfer is an important consideration in solution polymerizations. Chain transfer to solvent may reduce the rate of polymerization as well as the molecular weight of the polymer. Other chain-transfer reactions may iatroduce dye sites, branching, chromophoric groups, and stmctural defects which reduce thermal stabiUty. Many of the solvents used for acrylonitrile polymerization are very active in chain transfer. DMAC and DME have chain-transfer constants of 4.95-5.1 x lO " and 2.7-2.8 x lO " respectively, very high when compared to a value of only 0.05 x lO " for acrylonitrile itself DMSO (0.1-0.8 X lO " ) and aqueous zinc chloride (0.006 x lO " ), in contrast, have relatively low transfer constants hence, the relative desirabiUty of these two solvents over the former. DME, however, is used by several acryhc fiber producers as a solvent for solution polymerization. 

Components of a highly short chain branched (scb) waxymaize and a more long chain branched (Icb) amylomaize were separated on the semipreparative Sephacryl S-1000 system. Both samples contained high dp components that eluted in the exclusion volume, but the percentage of these components was quite different 90% for the scb waxymaize starch and approximately 10% for the Icb amylomaize starch (Fig. 16.6). The degree of polymerization averages for these samples was determined utilizing the previously established linear... 

Alkene polymerization can be carried out in a controlled manner using a Ziegler-Natta catalyst. Ziegler-Natta polymerization minimizes the amount of chain branching in the polymer and leads to stereoregular chains—either isotactic (substituents on the same side of the chain) or syndiotactic (substituents on alternate sides of the chain), rather than atactic (substituents randomly disposed). 

Sharkey, W. H. Polymerizations Through the Carbon-Sulphur Double Bond. VoL 17, pp. 73-103. Shimidzu, T. Cooperative Actions in the Nucleophile-Containing Polymers. Vol. 23, pp. 55-102. Slichter, W. P. The Study of High Polymers by Nuclear Magnetic Resonance. VoL 1, pp. 35-74. Small, P. A. Long-Chain Branching in Polymers. VoL 18,pp. 1-64. 

The presence of long chain branches in low density polyethylene (LDPE) accounts for the difference in properties e.g. higher melt strength, greater toughness for the same average molecular weight) between LDPE and linear low density polyethylene (LLDPE, made by coordination polymerization). 

Copolymerization of macromonomers formed by backbiting and fragmentation is a second mechanism for long chain branch formation during acrylate polymerization (Section 4.4.3.3). The extents of long and short chain branching in acrylate polymers in emulsion polymerization as a function of conditions have been quantified.20 ... 

It is also possible to prepare them from amino acids by the self-condensation reaction (3.12). The PAs (AABB) can be prepared from diamines and diacids by hydrolytic polymerization [see (3.12)]. The polyamides can also be prepared from other starting materials, such as esters, acid chlorides, isocyanates, silylated amines, and nitrils. The reactive acid chlorides are employed in the synthesis of wholly aromatic polyamides, such as poly(p-phenyleneterephthalamide) in (3.4). The molecular weight distribution (Mw/Mn) of these polymers follows the classical theory of molecular weight distribution and is nearly always in the region of 2. In some cases, such as PA-6,6, chain branching can take place and then the Mw/Mn ratio is higher. 

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